TY - JOUR
T1 - Sinonasal Biomarkers Defining Type 2-High and Type 2-Low Inflammation in Chronic Rhinosinusitis with Nasal Polyps
AU - De Corso, Eugenio
AU - Baroni, Silvia
AU - Settimi, Stefano
AU - Onori, Maria Elisabetta
AU - Troiani, Eliana
AU - Lucchetti, Donatella
AU - Montuori, Claudio
AU - Cantiani, Alessandro
AU - Porru, Davide Paolo
AU - Lo Verde, Simone
AU - Di Bella, Giuseppe Alberto
AU - Caruso, Cristiano
AU - Galli, Jacopo
PY - 2022
Y1 - 2022
N2 - The complex pathophysiology of chronic rhinosinusitis with nasal polyps (CRSwNP) generates a spectrum of phenotypes with a wide variety of inflammatory states. We enrolled 44 very-likely-to-be type 2 CRSwNP patients in order to evaluate the load of inflammation and to analyze human interleukins in nasal secretion. Clinical data were collected to evaluate the severity of the disease. High levels of IL-5, IL-4, IL-6, and IL-33 were detected in all type 2 CRSwNP patients. By analyzing type 2 cytokine profiles and local eosinophil count, we identified two coherent clusters: the first was characterized by high levels of IL-4, IL-5, IL-6, and a high-grade eosinophil count (type 2-high); the second had lower levels of cytokines and poor or absent eosinophilic inflammation (type-2 low). IL-5 levels were significantly higher within the type 2 cytokine and it was the most reliable biomarker for differentiating the two clusters. In type 2-high inflammatory profile clinical scores, the mean number of previous surgeries and need for systemic corticosteroids were significantly higher compared to type 2-low. Our research demonstrated the potential role of type 2 biomarkers, and in particular, of IL-5 in identifying patients with a more severe phenotype based on a high inflammatory load
AB - The complex pathophysiology of chronic rhinosinusitis with nasal polyps (CRSwNP) generates a spectrum of phenotypes with a wide variety of inflammatory states. We enrolled 44 very-likely-to-be type 2 CRSwNP patients in order to evaluate the load of inflammation and to analyze human interleukins in nasal secretion. Clinical data were collected to evaluate the severity of the disease. High levels of IL-5, IL-4, IL-6, and IL-33 were detected in all type 2 CRSwNP patients. By analyzing type 2 cytokine profiles and local eosinophil count, we identified two coherent clusters: the first was characterized by high levels of IL-4, IL-5, IL-6, and a high-grade eosinophil count (type 2-high); the second had lower levels of cytokines and poor or absent eosinophilic inflammation (type-2 low). IL-5 levels were significantly higher within the type 2 cytokine and it was the most reliable biomarker for differentiating the two clusters. In type 2-high inflammatory profile clinical scores, the mean number of previous surgeries and need for systemic corticosteroids were significantly higher compared to type 2-low. Our research demonstrated the potential role of type 2 biomarkers, and in particular, of IL-5 in identifying patients with a more severe phenotype based on a high inflammatory load
KW - biomarker
KW - chronic rhinosinusitis
KW - disease severity
KW - eosinophilic rhinitis
KW - medical therapy of chronic rhinosinusitis
KW - nasal polyposis
KW - biomarker
KW - chronic rhinosinusitis
KW - disease severity
KW - eosinophilic rhinitis
KW - medical therapy of chronic rhinosinusitis
KW - nasal polyposis
UR - http://hdl.handle.net/10807/231001
U2 - 10.3390/jpm12081251
DO - 10.3390/jpm12081251
M3 - Article
SN - 2075-4426
VL - 12
SP - 1251
EP - 1251
JO - Journal of Personalized Medicine
JF - Journal of Personalized Medicine
ER -